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8321. Pilot Project on External Vestibular Prosthesis in Chronic Subjective Dizziness

to be influencing the symptoms reported beyond the CSD alone. Patients with mobility restriction that would prevent participating in the tests or the intensive therapy trials. Subjects with hearing impairment that interferes with oral communication. Contacts and Locations Go to Information from the National Library of Medicine To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor. Please refer to this study by its (...) this error by providing patients with reliable motion stimuli. Condition or disease Intervention/treatment Phase Dizziness Chronic Device: Balance Belt Not Applicable Study Design Go to Layout table for study information Study Type : Interventional (Clinical Trial) Estimated Enrollment : 30 participants Intervention Model: Single Group Assignment Masking: None (Open Label) Primary Purpose: Treatment Official Title: A Pilot Project to Investigate the Use of an External Vestibular Prosthesis Potential

2014 Clinical Trials

8322. The Effect of Dietary Strawberry Supplementation on Older Adults

Aging Age-related Memory Disorders Dietary Supplement: Freeze-dried Strawberry Dietary Supplement: Strawberry Placebo Not Applicable Detailed Description: This study is being conducted to assess the effect of dietary strawberry supplementation vs. placebo on measures of cognition and mobility in older adults. Participants will visit the HNRCA on 4 occasions. During the first visit, participants will complete a dietary assessment and familiarize themselves with some of the cognitive tests used (...) Information provided by (Responsible Party): Barbara Shukitt-Hale, USDA Human Nutrition Research Center on Aging Study Details Study Description Go to Brief Summary: This study is being conducted to assess the effect of dietary strawberry supplementation on cognition and mobility in older adults. It is hypothesized that plant compounds, present in strawberries, may improve cognition and mobility by protecting against oxidative stress and inflammation. Condition or disease Intervention/treatment Phase

2014 Clinical Trials

8323. Intensive Diet and Exercise or Standard of Care in Improving Physical Function and Quality of Life in Patients With Prostate Cancer Undergoing Androgen Deprivation Therapy

than standard of care in improving physical function and quality of life in patients with prostate cancer undergoing androgen deprivation therapy. Condition or disease Intervention/treatment Phase Recurrent Prostate Cancer Stage IV Prostate Cancer Behavioral: behavioral dietary intervention Behavioral: exercise intervention Other: behavioral activity counseling Behavioral: telephone based counseling Procedure: quality-of-life assessment Other: questionnaire administration Not Applicable Detailed (...) of a Lifestyle Intervention in Men Undergoing Androgen Deprivation Therapy Study Start Date : April 2012 Actual Primary Completion Date : May 2015 Resource links provided by the National Library of Medicine related topics: related topics: Arms and Interventions Go to Arm Intervention/treatment Experimental: Arm I (diet and exercise intervention) EXERCISE COMPONENT: Patients undergo 1 hour of monitored intensive exercise comprising 30 minutes of aerobic exercise and 30 minutes of resistance exercise twice

2014 Clinical Trials

8324. Assessing the Impact of an Intervention to Prevent Intimate Partner Violence and HIV in Uganda

community services alone. Hypothesis 3(a): Incidence of HIV will be lower in the intervention vs. control arms. Condition or disease Intervention/treatment Phase HIV Physical Abuse of Adult (If Focus of Attention is on Victim) Sexual Abuse of Adult (If Focus of Attention is on Victim) Risk Reduction Behavior Behavioral: The SHARE Project Not Applicable Study Design Go to Layout table for study information Study Type : Interventional (Clinical Trial) Actual Enrollment : 11451 participants Allocation (...) of Medicine related topics: Arms and Interventions Go to Arm Intervention/treatment Experimental: Intervention arm Intervention arm clusters (n=4) received an IPV prevention intervention (the Safe Homes and Respect for Everyone (SHARE) Project), enhanced HIV testing and treatment and routine HIV services. Behavioral: The SHARE Project SHARE aimed to reduce IPV and used methodologies from two proven successful violence prevention frameworks: Stepping Stones (Welbourn, 1995) and the Resource Guide

2014 Clinical Trials

8325. Short Messaging Service for Optimizing Hemoglobin A1C Management in Low-Income Diabetics

Not Applicable Detailed Description: This multi-center, unblinded, prospective randomized controlled trial will enroll adult diabetic patients of the Wilson Community Health Center, Harvest Family Health Center, and Freedom Hill Community Health Center living below 200% of 2013 poverty level with a serum hemoglobin A1C >9% and who currently own a mobile device with text messaging capacity. After written informed consent has been obtained, subjects will be randomized to intervention or control group (1:1 (...) ), stratified based on insulin initiation within 1 week of study inclusion. Participants randomized to the intervention group will be further divided into subgroups as "insulin user" or "non-insulin user" and both will receive SMS messages every 7 days. The content of the message consist of medication reminders, reporting of blood glucose results, insulin technique assessment (if applicable), or d) medication adherence assessment. Participants will be asked to respond with a simple text within 7 days

2014 Clinical Trials

8326. Study Protocol Comparing Polidocanol Versus Hypertonic Glucose for Treatment of Reticular Veins

that may be related to the study drugs any cause of dermatitis on application site free of comorbidities clinically serious as diabetes mellitus, heart failure, respiratory failure, uncontrolled hypertension with medication, and uncontrolled hypothyroidism pregnancy previous deep vein thrombosis (DVT) family history of DVT thrombophilia do not agree with the search terms Contacts and Locations Go to Information from the National Library of Medicine To learn more about this study, you or your doctor may (...) in Treatment of Reticular Veins at the Lower Limbs. Study Start Date : September 2012 Actual Primary Completion Date : December 2014 Actual Study Completion Date : December 2014 Resource links provided by the National Library of Medicine related topics: available for: Arms and Interventions Go to Arm Intervention/treatment Active Comparator: Polidocanol with Glucose An application session 0.2% Polidocanol + 70% Glucose to treat reticular veins of the lower limb selected, with a maximum volume of 5 ml. Drug

2014 Clinical Trials

8327. Effect of Short Message Service Intervention on Stent Removal/Exchange Adherence in Patients With Benign Pancreaticobiliary Diseases

that patients with stent implantation did not follow the recommendation of further stent management by endoscopists. Many methods have been used to improve the adherence of patients in medical service. With the advance of mobile technology and popular use of mobile phones, it was believed that the patient-centered outcome could be improved by mobile telecommunication with the timely support of a patient by a health professional. Thus we hypothesize that mobile technology, reminding the patients (...) Recruitment Status : Completed First Posted : January 22, 2014 Last Update Posted : January 22, 2014 Sponsor: Fourth Military Medical University Information provided by (Responsible Party): Yanglin Pan, Fourth Military Medical University Study Details Study Description Go to Brief Summary: Endoscopic implantation of plastic or covered metal stents is widely used in a variety of benign pancreaticobiliary diseases, including duct stricture, large or difficult stones, bile or pancreatic juice leak, etc

2014 Clinical Trials

8328. CBT Through Internet and Smartphones for Adults With ADHD

therapy (iCBT) with an additional smartphone application and evaluated through a randomized controlled trial during 12 weeks. The patients will be randomized to one of three conditions an active treatment group where the intervention is based on cognitive - and dialectical behavioral therapy (CBT and DBT) and the mobile app. an active ICBT-treatment based on psychoeducation, a CBT stress-reduction program and Applied Relaxation, and treatment as usual (TAU) / waiting list. The main objective (...) : Internet stress-reduction Other: Treatment as usual (TAU)/waiting list Not Applicable Detailed Description: Approximately one-third of children with ADHD continue to be fully symptomatic into adulthood and many of the remainders often retain some residual problems that require treatment. Thus ADHD is a prevalent and chronic disabling disorder. Drugs provide first line treatment for adults with ADHD but are not enough for everybody, while we still lack proper evidence for promising psychological

2014 Clinical Trials

8329. Mindfulness-based Cognitive Therapy for Chronic Obstructive Pulmonary Disease

Volunteers: No Criteria Inclusion Criteria: severe to very severe COPD motivated to participate in pulmonary rehabilitation sufficient mobility to attend pulmonary rehabilitation Exclusion Criteria: certain comorbidities (e.g. unstable coronary complications, psychiatric illness) severe cognitive disability (e.g. dementia) inability to speak Danish Contacts and Locations Go to Information from the National Library of Medicine To learn more about this study, you or your doctor may contact the study (...) (COPD) Chronic Obstructive Lung Disease Chronic Obstructive Airway Disease Chronic Bronchitis Emphysema Behavioral: Mindfulness-based cognitive therapy Behavioral: Pulmonary rehabilitation Not Applicable Detailed Description: Chronic obstructive pulmonary disease (COPD) is a major burden for the affected patients, who are continuously struggling with the hallmark symptoms breathlessness, cough, and sputum together with high levels of anxiety and depression and impairment of quality of life (QoL

2014 Clinical Trials

8330. A Clinical Study of Two Dentinal Hypersensitivity Treatments Used With Normal Oral Hygiene

Information provided by (Responsible Party): Procter and Gamble Study Details Study Description Go to Brief Summary: This study will compare the safety and effectiveness of normal oral hygiene with two different marketed dentifrices, on longer term dentinal hypersensitivity response following use of potassium oxalate desensitizers. Condition or disease Intervention/treatment Phase Dentin Sensitivity Device: Potassium oxalate Drug: Sodium fluoride paste Drug: Stannous fluoride paste Not Applicable Study (...) Completion Date : October 2014 Resource links provided by the National Library of Medicine related topics: available for: Arms and Interventions Go to Arm Intervention/treatment oxalate liquid & gel plus SnF2 paste Potassium oxalate liquid, professionally applied Potassium oxalate gel, self applied Stannous fluoride paste, self applied Device: Potassium oxalate Professionally applied (liquid) and self applied (gel) Drug: Stannous fluoride paste Toothpaste used by subject Other Name: SnF2 paste oxalate

2014 Clinical Trials

8331. Mulligan Concept Mobilisation With Movement for Shoulder Dysfunction in Older Adults

provided by (Responsible Party): Cristina Lirio Romero, University of Alcala Study Details Study Description Go to Brief Summary: Objective: To pilot the methods proposed for conducting a full randomised clinical trial to evaluate the effect of Mulligan concept mobilization with movement on shoulder functionality in older adults with shoulder dysfunction. Design: Pilot randomised, single-blinded clinical trial. Setting: Three nursing homes, Toledo, Spain. Participants: 44 older adults with shoulder (...) -SDQ) Spanish version, and secondary outcomes are active glenohumeral range of motion and pain intensity. Data will be collected at baseline, after each group intervention, and 1 and 3 months after finishing interventions. Condition or disease Intervention/treatment Phase Disorder of Shoulder Other: Standard protocol Other: Mulligan Concept Mobilisation with Movement Not Applicable Detailed Description: Shoulder dysfunction is a common problem in older adults reaching up to 21% of prevalence

2014 Clinical Trials

8332. The Survival Rate of Glass Ionomer Cement, Glass Carbomer Cement and Compomer in Occlusal and Proximal ART Restorations

, the dentists preferred side, the child's dmft/DMFT, contamination and finally the preoperative conditions. The effect of these variables on the survival rate will be evaluated using a regression analysis. Condition or disease Intervention/treatment Phase Caries Involving Multiple Surfaces of Tooth Dental Caries on Chewing Surface of Tooth Dental Caries Extending Into Dentine Procedure: GIC Restorations Procedure: Carbomer Restorations Procedure: Compomer Restorations Not Applicable Detailed Description (...) , 2018 Resource links provided by the National Library of Medicine related topics: available for: Arms and Interventions Go to Arm Intervention/treatment Active Comparator: GIC Restorations Restorations using Glass Ionomer Cement Procedure: GIC Restorations Restorations using Glass Ionomer Cement Experimental: Compomer Restorations Restorations using Compomer Procedure: Compomer Restorations Restorations using Compomer Experimental: Carbomer Restorations Restorations using Glass Carbomer Procedure

2014 Clinical Trials

8333. Effects of Facility-based Mother Support Groups on Prevention of mother-to Child Transmission Outcomes in Zimbabwe

2 consists of standard of care together with facility-based MSGs. Condition or disease Intervention/treatment Phase HIV Infection Behavioral: Mother support groups for HIV+ mothers Not Applicable Detailed Description: PRIMARY OBJECTIVE To test whether MSGs lead to increased retention of HIV-exposed infants in PMTCT programmes SECONDARY OBJECTIVES To assess whether MSGs lead to increased retention of mothers in postnatal HIV follow-up care To assess whether male participation in PMTCT activities (...) will be entered, coded, cleaned and locked before analyses are made. Data will be analysed on an intention-to-treat basis. A mobile team of well-trained quality assurance and control study staff will be deployed throughout the data collection period to ensure quality of the intervention and of data generated and collected at each study site. A pre-specified proportion of patient visit records will be reviewed from each site. Study Design Go to Layout table for study information Study Type : Interventional

2014 Clinical Trials

8334. Developing a Smartphone App With Mindfulness Training for Teen Smoking Cessation

of Massachusetts Medical School Worcester, Massachusetts, United States, 01655 Sponsors and Collaborators University of Massachusetts, Worcester Investigators Layout table for investigator information Principal Investigator: Lori Pbert, PhD University of Massachusetts, Worcester Principal Investigator: Judson Brewer, MD University of Massachusetts, Worcester More Information Go to Layout table for additonal information Responsible Party: Lori Pbert, Professor of Medicine, University of Massachusetts, Worcester (...) Behavioral: Written smoking cessation materials only Not Applicable Detailed Description: The new Surgeon General's Report (SGR), Preventing Tobacco Use Among Youth and Young Adults, highlights the addictive nature of nicotine and emphasizes the need for effective and accessible cessation treatment for the more than 3.6 million youth who smoke. This proposal is in response to PA-13-078, Behavioral and Integrative Treatment Development Program (R34), which supports the development and testing

2014 Clinical Trials

8335. Abdominal Circumference and Cardiorespiratory Repercussions in Patients Submitted to Physical Therapy

chest physiotherapy. [ Time Frame: Baseline, five and thirty minutes. ] Heart rate variability has become the conventionally accepted term to describe variations of both instantaneous heart rate and intervals (time domain). Thoracoabdominal perimetry consists of a set of measurements of thoracic and abdominal circumferences during respiratory movements, and it aims at quantifying the thoracoabdominal mobility. Eligibility Criteria Go to Information from the National Library of Medicine Choosing (...) wall expansion Other: Chest physiotherapy airway clearance modality Not Applicable Detailed Description: The physiotherapist assessment will consist of anthropometry (body mass index, abdominal circumference, adipometer); chest inspection and palpation, vital signs (blood pressure, heart rate, respiratory frequence, oxymetry), dyspnea index and capillar blood glucose; and later with pulmonary tests (thoracoabdominal perimetry, respiratory muscle strength and pulmonary volume and capacity

2014 Clinical Trials

8336. Exercise in Pediatric Cancer Patient Undergoing Anti-Cancer Treatment

and balance capacity (TUDS, one leg stand), postural control functional mobility (posturomed & force plate), range of motion (goniometer) Quality of Life [ Time Frame: after primary treatment (6 month) and after one year ] KINDL questionnaire Feasibility between 6 and 12 month [ Time Frame: between end of primary treatment (6 month) and one year ] Will be measured as the proportion of patients following the exercise prescription. Eligibility Criteria Go to Information from the National Library of Medicine (...) Heidelberg Heidelberg University University of Leipzig Children`s Medical Hospital, University of Leipzig, Leipzig, Germany Information provided by (Responsible Party): German Cancer Research Center Study Details Study Description Go to Brief Summary: Today about 80% childhood cancer patients become long-time survivors. In spite of the high cure rates the diagnosis cancer is associated with a variety of disease and treatment-related psychological and physical impairments mostly present into adulthood. So

2014 Clinical Trials

8337. The Effect of Acetaminophen on Non-alcoholic Fatty Liver Disease Patients

: Presence of the metabolic syndrome, defined according to the modified AHA/NCEP criteria Taking concomitant medications Contacts and Locations Go to Information from the National Library of Medicine To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor. Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02194894 Locations Layout table for location information United States, California (...) , and/or eosinophilia (>5%). We follow a conservative approach derived from the FDA guidelines for stopping medications expected to cause drug induced liver injury (DILI). Indeed, the FDA allows continuation of the medication until ALT or AST are >8x ULN in the absence of elevated Tbili or INR. Patients who have hepatotoxicity will have close monitoring of their liver enzymes until they normalize. Taking acetaminophen up to 3g daily has been shown to be safe and acceptable. We have followed very strict criteria

2014 Clinical Trials

8338. A Trial of Rehabilitation Therapy in Older Acute Heart Failure Patients

and 3 months ] Secondary Outcome Measures : All-Cause rehospitalization [ Time Frame: 6 months from index hospital discharge ] Other Outcome Measures: Economic Analysis [ Time Frame: 6-months ] Assess the economic impact of the intervention by comparing medical costs between treatment arms, inclusive of the cost for rehabilitation therapy, relative to its associated changes in health outcomes. Eligibility Criteria Go to Information from the National Library of Medicine Choosing to participate (...) participating in formal, facility-based cardiac rehabilitation Contacts and Locations Go to Information from the National Library of Medicine To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor. Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02196038 Locations Layout table for location information United States, North Carolina Duke University Medical Center Recruiting Durham, North

2014 Clinical Trials

8339. Randomized Clinical Trial of Enamel Matrix Derivative: Radiographic Analysis

radiographs at baseline and after 24 months. Images were digitized and used to measure the distances from the cemento-enamel junction (CEJ) to the alveolar crest (AC), CEJ to the bottom of the defect (BD) and infrabony defect angle. Condition or disease Intervention/treatment Phase Chronic Periodontitis Drug: enamel matrix derivative Procedure: Open flap debridement Not Applicable Study Design Go to Layout table for study information Study Type : Interventional (Clinical Trial) Actual Enrollment : 48 (...) ) Eligibility Criteria Go to Information from the National Library of Medicine Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Layout table for eligibility information Ages Eligible for Study: 18 Years and older (Adult, Older Adult) Sexes Eligible for Study

2014 Clinical Trials

8340. Hypoxia and Exercise in the Elderly

is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT02196623 Recruitment Status : Completed First Posted : July 22, 2014 Last Update Posted : January 24, 2019 Sponsor: Hannover Medical School Collaborator: German Diabetes Center Information provided by (Responsible Party): Hannover Medical School Study Details Study Description Go to Brief Summary: Ageing (...) is the primary risk factor for most chronic diseases including type 2 diabetes mellitus. Sarcopenia and muscular mitochondrial dysfunction with aging are crucial mechanisms leading to decreased exercise tolerance and worsened insulin sensitivity. Thus, metabolic disease and frailty, which limits physical mobility as well as quality of life, share common cellular mechanisms. The investigators will test the hypothesis that a combination of normobaric hypoxia and exercise training elicits a synergistic effect

2014 Clinical Trials

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